TY - JOUR
T1 - Greater Early Posttrauma Activation in the Right Inferior Frontal Gyrus Predicts Recovery From Posttraumatic Stress Disorder Symptoms
AU - Sheynin, Jony
AU - Lokshina, Yana
AU - Ahrari, Samira
AU - Nickelsen, Tetiana
AU - Duval, Elizabeth R.
AU - Ben-Zion, Ziv
AU - Shalev, Arieh Y.
AU - Hendler, Talma
AU - Liberzon, Israel
N1 - Funding Information:
This work was supported by the National Institute of Mental Health (Grant No. R01-MH-103287 [to AYS, IL, and TH]). The views expressed in this article are solely those of the authors and do not reflect an endorsement by or the official policy of the Department of Veterans Affairs, the Department of Defense, or the U.S. government, or the official views of the National Institutes of Health. We thank Mike Angstadt for assistance with MRI data analysis, as well as the research team at Tel-Aviv Sourasky Medical Center (Naomi Fine, Nili Green, Mor Halevi, Sheli Luvton, Yael Shavit, Olga Nevenchannaya, Iris Rashap, Efrat Routledge, and Ophir Leshets) for assistance with participants screening, enrollment, assessment, and follow-up. We also extend our gratitude to all the participants of this study, who completed the assessments at multiple time points after experiencing a traumatic event, thus contributing to scientific research on posttraumatic psychopathology. Presented at the Society of Biological Psychiatry annual meeting, April 28–30, 2022, New Orleans, Louisiana. The authors report no biomedical financial interests or potential conflicts of interest. ClinicalTrials.gov: Neurobehavioral Moderators of Post-traumatic Disease Trajectories; https://www.clinicaltrials.gov/study/NCT03756545; NCT03756545.
Funding Information:
This work was supported by the National Institute of Mental Health (Grant No. R01-MH-103287 [to AYS, IL, and TH]). The views expressed in this article are solely those of the authors and do not reflect an endorsement by or the official policy of the Department of Veterans Affairs, the Department of Defense, or the U.S. government, or the official views of the National Institutes of Health.
Publisher Copyright:
© 2023 Society of Biological Psychiatry
PY - 2024/1
Y1 - 2024/1
N2 - Background: Posttraumatic stress disorder (PTSD) has been associated with altered emotion processing and modulation in specific brain regions, i.e., the amygdala, insula, and medial prefrontal and anterior cingulate cortices. Functional alterations in these regions, recorded shortly after trauma exposure, may predict changes in PTSD symptoms. Methods: Survivors (N = 104) of a traumatic event, predominantly a motor vehicle accident, were included. Functional magnetic resonance imaging was used to assess brain activation 1, 6, and 14 months after trauma exposure (T1, T2, and T3, respectively). Participants performed the Shifted-attention Emotional Appraisal Task, which probes 3 affective processes: implicit emotional processing (of emotional faces), emotion modulation by attention shifting (away from these faces), and emotion modulation by appraisal (of the participants’ own emotional response to these faces). We defined regions of interest based on task-related activations, extracted beta weights from these regions of interest, and submitted them to a series of analyses to examine relationships between neural activation and PTSD severity over the 3 time points. Results: At T1, a regression model containing activations in the left dorsolateral prefrontal cortex, bilateral inferior frontal gyrus (IFG), and medial prefrontal cortex during emotion modulation by appraisal significantly predicted change in PTSD symptoms. More specifically, greater right IFG activation at T1 was associated with greater reduction in symptom severity (T1–T3). Exploratory analysis also found that activation of the right IFG increased from T1 to T3. Conclusions: The results suggest that greater early posttrauma activation during emotion appraisal in the right IFG, a region previously linked to cognitive control in PTSD, predicts recovery from PTSD symptoms.
AB - Background: Posttraumatic stress disorder (PTSD) has been associated with altered emotion processing and modulation in specific brain regions, i.e., the amygdala, insula, and medial prefrontal and anterior cingulate cortices. Functional alterations in these regions, recorded shortly after trauma exposure, may predict changes in PTSD symptoms. Methods: Survivors (N = 104) of a traumatic event, predominantly a motor vehicle accident, were included. Functional magnetic resonance imaging was used to assess brain activation 1, 6, and 14 months after trauma exposure (T1, T2, and T3, respectively). Participants performed the Shifted-attention Emotional Appraisal Task, which probes 3 affective processes: implicit emotional processing (of emotional faces), emotion modulation by attention shifting (away from these faces), and emotion modulation by appraisal (of the participants’ own emotional response to these faces). We defined regions of interest based on task-related activations, extracted beta weights from these regions of interest, and submitted them to a series of analyses to examine relationships between neural activation and PTSD severity over the 3 time points. Results: At T1, a regression model containing activations in the left dorsolateral prefrontal cortex, bilateral inferior frontal gyrus (IFG), and medial prefrontal cortex during emotion modulation by appraisal significantly predicted change in PTSD symptoms. More specifically, greater right IFG activation at T1 was associated with greater reduction in symptom severity (T1–T3). Exploratory analysis also found that activation of the right IFG increased from T1 to T3. Conclusions: The results suggest that greater early posttrauma activation during emotion appraisal in the right IFG, a region previously linked to cognitive control in PTSD, predicts recovery from PTSD symptoms.
KW - Emotion appraisal
KW - Emotion processing and modulation
KW - IFG
KW - PTSD
KW - Trauma
KW - fMRI
KW - Brain
KW - Stress Disorders, Post-Traumatic
KW - Amygdala
KW - Humans
KW - Emotions/physiology
KW - Prefrontal Cortex/diagnostic imaging
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U2 - 10.1016/j.bpsc.2023.07.002
DO - 10.1016/j.bpsc.2023.07.002
M3 - Article
C2 - 37451548
AN - SCOPUS:85174063049
SN - 2451-9022
VL - 9
SP - 91
EP - 100
JO - Biological Psychiatry: Cognitive Neuroscience and Neuroimaging
JF - Biological Psychiatry: Cognitive Neuroscience and Neuroimaging
IS - 1
ER -